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HRID 403031作成日:2026年10月26日

Potassium Carbonate → N-cyclopropyl-4-methyl-3-({4-[(3-methylpyridin-2-yl)methoxy]benzoyl}amino)benzamide

https://huagongshe.com/reaction/403031

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物Thionyl ChlorideHCID 24386—
反応物(3-Methylpyridin-2-yl)methanolHCID 1514369—
反応物N-cyclopropyl-3-[(4-hydroxybenzoyl)amino]-4-methylbenzamideHCID 66631169—
溶媒AcetonitrileHCID 6342—
溶媒DichloromethaneHCID 6344—
生成物N-cyclopropyl-4-methyl-3-({4-[(3-methylpyridin-2-yl)methoxy]benzoyl}amino)benzamideHCID 11165932102.2%

反応条件

温度80 °C

反応手順

To (3-methylpyridine-2-yl)methanol (157 mg, 1.272 mmol) in DCM (5 mL) was added thionyl chloride (200 μl) and the mixture stirred and heated at reflux for 4 h. The mixture was evaporated to dryness. To the residue was added N-cyclopropyl-3-[(4-hydroxybenzoyl)amino]-4-methylbenzamide (197 mg, 0.636 mmol) and potassium carbonate (176 mg, 1.27 mmol) in acetonitrile (5 mL) and the resulting mixture heated at 80° C. for 16 h. The reaction mixture was cooled and partitioned between saturated aqueous sodium bicarbonate and ethyl acetate. The organic phase was concentrated under reduced pressure. Precipitation with DCM in diethyl ether gave the title compound as a solid (270 mg); NMR Spectrum: (DMSOd6) 0.57 (m, 2H), 0.68 (m, 2H), 2.26 (s, 3H), 2.40 (s, 3H), 2.86 (m, 1H), 5.30 (s, 2H), 7.17 (d, 2H), 7.33 (m, 2H), 7.65 (m, 2H), 7.82 (s, 1H), 7.97 (d, 2H), 8.39 (m, 2H), 9.81 (s, 1H); Mass Spectrum: M+H+ 416.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08742124B2
出典データセットuspto-grants-2014_06
ORD IDord-5edb858c26bf4de9bbd8fb6bd245c791
出典メモuspto-grants-2014_06